Triethylamine → Benzoic acid, 5-ethyl-2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester

To 3.0 g (16.6 mmol) of methyl 5-ethyl-2-hydroxybenzoate in 100 mL of CH2Cl2 at 0° C. was added 5.8 mL (41.5 mmol, 2.5 eq.) of Et3N. To this stirred solution was added dropwise 3.6 mL (21.6 mmol, 1.3 eq.) of Tf2O. Following complete addition 0.2 g (cat.) of 4-dimethylamino pyridine was added and the reaction mixture was allowed to warm to room temperature. After 4 h stirring at this temperature the reaction was judged complete, and quenched by the addition of a saturated aqueous solution of NaHCO3 (100 mL). The resulting layers were separated and the aqueous layer extracted twice with CH2Cl2 (100 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The resulting residue was purified by column chromatography to yield the desired methyl 5-ethyl-2-{[(trifluoromethyl)sulfonyl]oxy}benzoate. 1H NMR (400 MHz, CDCl3): δ=7.94 (d, J=2.3 Hz, 1H), 7.47 (dd, J=2.3, 8.4 Hz, 1H), 7.24 (d, J=8.4 Hz, 1H), 4.00 (s, 3H), 2.76 (q, J=7.6 Hz, 2H), 1.28 (t, J=7.6 Hz, 3H).

1. additionwas added
2. customquenched by the addition of a saturated aqueous solution of NaHCO3 (100 mL)
3. customThe resulting layers were separated
4. extractionthe aqueous layer extracted twice with CH2Cl2 (100 mL)
5. dry with materialThe combined organic layers were dried over MgSO4
6. filtrationfiltered
7. concentrationconcentrated under reduced pressure
8. customThe resulting residue was purified by column chromatography

ORD record

ord-f085bbc2c5fb4320b5ce82c12f10f870

Source dataset

uspto-grants-2010_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07645780B2